Allele Registry

Canonical Allele Identifier: PA645460757

Gene: GCK HGNC NCBI

ClinVar RCV:

RCV002281721

ClinVar Variation:

36178

HGVS (amino-acid)	Matching Registered Transcripts
NP_277042.1:p.Met382Arg	CA213719 NM_033507.3:c.1145T>G